Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To

Clinical Features

Phenotypes and symptoms related to Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To

  • Peripheral neuropathy
  • Visual loss
  • Apnea
  • Hypercholesterolemia
  • Sleep apnea
  • Optic neuropathy
  • Drusen
  • Nonarteritic anterior ischemic optic neuropathy
  • Optic disc drusen

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To Is also known as naion, susceptibility to, optic neuropathy, anterior ischemic, susceptibility to.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Platelet Disorders.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

RUNX1, STIM1, TBXA2R, TBXAS1, USF1, VPS33B, VWF, WAS, GP6, HPS3, HPS4, CD36, HPS5, DTNBP1, P2RY12, HPS6, MASTL, LYST, VIPAS39, FERMT3 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
100 %
Thrombocytopenia Sequencing Panel.

By Genetic Services Laboratory University of Chicago (United States).

CFB, SRC, TERC, TERT, THBD, VWF, WAS, C3, ADAMTS13, ABCG5, ABCG8, RUNX1T1, TUBB1, ACTN1, CFHR4, CFHR3, CYCS, CFHR5, DGKE, ANKRD26 , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
100 %
Thrombocytopenia Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago (United States).

CFB, RUNX1, SRC, TERC, TERT, THBD, VWF, WAS, C3, ADAMTS13, ABCG5, ABCG8, TUBB1, ACTN1, CFHR4, CFHR3, CYCS, CFHR5, DGKE, ANKRD26 , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
100 %
Bernard Soulier Syndrome.

By Institute of Human Genetics Uniklinik RWTH Aachen (Germany).

GP1BA, GP1BB, GP9
Specificity
34 %
Genes
100 %
VWD Platelet Type (GP1BA) 4 Mutations.

By ARUP Laboratories, Molecular Genetics and Genomics (United States).

GP1BA
Specificity
100 %
Genes
100 %
Bernard-Soulier syndrome.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust (United Kingdom).

GP1BA, GP1BB, GP9
Specificity
34 %
Genes
100 %
GP1BA. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

GP1BA
Specificity
100 %
Genes
100 %
Bernard-Soulier syndrome (sequence analysis of GP1BA gene).

By CGC Genetics (Portugal).

GP1BA
Specificity
100 %
Genes
100 %

You can get up to 51 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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